Leber Congenital Amaurosis (LCA) (Ophthalmology) - Drugs In Development, 2021

July 2021 | 82 pages | ID: L717FC9A00A3EN
Global Markets Direct

Abstracts

Leber Congenital Amaurosis (LCA) (Ophthalmology) - Drugs In Development, 2021

SUMMARY

Global Markets Direct's latest Pharmaceutical and Healthcare disease pipeline guide Leber Congenital Amaurosis - Drugs In Development, 2021, provides an overview of the Leber Congenital Amaurosis (Genetic Disorders) pipeline landscape.

Leber congenital amaurosis is an eye disorder that primarily affects the retina, which is the specialized tissue at the back of the eye that detects light and color. This condition is the most common cause of inherited blindness in childhood. Symptoms include vision loss, roving eye movements, deep-set eyes, developmental delay, epilepsy, and motor skill impairment.

REPORT HIGHLIGHTS

Global Markets Direct's Pharmaceutical and Healthcare latest pipeline guide Leber Congenital Amaurosis - Drugs In Development, 2021, provides comprehensive information on the therapeutics under development for Leber Congenital Amaurosis (Genetic Disorders), complete with analysis by stage of development, drug target, mechanism of action (MoA), route of administration (RoA) and molecule type. The guide covers the descriptive pharmacological action of the therapeutics, its complete research and development history and latest news and press releases.

The Leber Congenital Amaurosis (Genetic Disorders) pipeline guide also reviews of key players involved in therapeutic development for Leber Congenital Amaurosis (LCA) and features dormant and discontinued projects. The guide covers therapeutics under Development by Companies/Universities/Institutes, the molecules developed by Companies in Phase III, Phase II, Preclinical and Discovery stages are 1, 3, 7 and 2 respectively. Similarly, the Universities portfolio in Phase I, Preclinical and Discovery stages comprises 2, 2 and 1 molecules, respectively.

Leber Congenital Amaurosis (Genetic Disorders) pipeline guide helps in identifying and tracking emerging players in the market and their portfolios, enhances decision making capabilities and helps to create effective counter strategies to gain competitive advantage. The guide is built using data and information sourced from Global Markets Direct’s proprietary databases, company/university websites, clinical trial registries, conferences, SEC filings, investor presentations and featured press releases from company/university sites and industry-specific third party sources. Additionally, various dynamic tracking processes ensure that the most recent developments are captured on a real time basis.

Note: Certain content/sections in the pipeline guide may be removed or altered based on the availability and relevance of data.

SCOPE

• The pipeline guide provides a snapshot of the global therapeutic landscape of Leber Congenital Amaurosis (Genetic Disorders).
• The pipeline guide reviews pipeline therapeutics for Leber Congenital Amaurosis (Genetic Disorders) by companies and universities/research institutes based on information derived from company and industry-specific sources.
• The pipeline guide covers pipeline products based on several stages of development ranging from pre-registration till discovery and undisclosed stages.
• The pipeline guide features descriptive drug profiles for the pipeline products which comprise, product description, descriptive licensing and collaboration details, R&D brief, MoA & other developmental activities.
• The pipeline guide reviews key companies involved in Leber Congenital Amaurosis (Genetic Disorders) therapeutics and enlists all their major and minor projects.
• The pipeline guide evaluates Leber Congenital Amaurosis (Genetic Disorders) therapeutics based on mechanism of action (MoA), drug target, route of administration (RoA) and molecule type.
• The pipeline guide encapsulates all the dormant and discontinued pipeline projects.
• The pipeline guide reviews latest news related to pipeline therapeutics for Leber Congenital Amaurosis (Genetic Disorders)

REASONS TO BUY

• Procure strategically important competitor information, analysis, and insights to formulate effective R&D strategies.
• Recognize emerging players with potentially strong product portfolio and create effective counter-strategies to gain competitive advantage.
• Find and recognize significant and varied types of therapeutics under development for Leber Congenital Amaurosis (Genetic Disorders).
• Classify potential new clients or partners in the target demographic.
• Develop tactical initiatives by understanding the focus areas of leading companies.
• Plan mergers and acquisitions meritoriously by identifying key players and it’s most promising pipeline therapeutics.
• Formulate corrective measures for pipeline projects by understanding Leber Congenital Amaurosis (Genetic Disorders) pipeline depth and focus of Indication therapeutics.
• Develop and design in-licensing and out-licensing strategies by identifying prospective partners with the most attractive projects to enhance and expand business potential and scope.
• Adjust the therapeutic portfolio by recognizing discontinued projects and understand from the know-how what drove them from pipeline.

Contents

Introduction
Global Markets Direct Report Coverage
Leber Congenital Amaurosis (LCA) - Overview
Leber Congenital Amaurosis (LCA) - Therapeutics Development
Pipeline Overview
Pipeline by Companies
Pipeline by Universities/Institutes
Products under Development by Companies
Products under Development by Universities/Institutes
Leber Congenital Amaurosis (LCA) - Therapeutics Assessment
Assessment by Target
Assessment by Mechanism of Action
Assessment by Route of Administration
Assessment by Molecule Type
Leber Congenital Amaurosis (LCA) - Companies Involved in Therapeutics Development
Atsena Therapeutics Inc
Editas Medicine Inc
Generation Bio Co
IVERIC bio Inc
MeiraGTx Holdings Plc
Ocugen Inc
Odylia Therapeutics Inc
Oxford BioMedica Plc
ProQR Therapeutics NV
Variant
Leber Congenital Amaurosis (LCA) - Drug Profiles
AAV-AIPL1 - Drug Profile
Product Description
Mechanism Of Action
R&D Progress
cevaretigene ritoparvovec - Drug Profile
Product Description
Mechanism Of Action
R&D Progress
EDIT-101 - Drug Profile
Product Description
Mechanism Of Action
R&D Progress
Gene Therapy for Leber’s Congenital Amaurosis, Stargardt Disease And Wet Age-related Macular Degeneration - Drug Profile
Product Description
Mechanism Of Action
R&D Progress
Gene Therapy to Activate CEP290 for Leber Congenital Amaurosis - Drug Profile
Product Description
Mechanism Of Action
R&D Progress
Gene Therapy to Activate CRX for Leber Congenital Amaurosis - Drug Profile
Product Description
Mechanism Of Action
R&D Progress
Gene Therapy to Activate Retinal Guanylyl Cyclase-1 for Leber Congenital Amaurosis-1 - Drug Profile
Product Description
Mechanism Of Action
R&D Progress
Gene Therapy to Activate RPE65 for Leber Congenital Amaurosis - Drug Profile
Product Description
Mechanism Of Action
R&D Progress
Gene Therapy to Activate RPE65 for Leber Congenital Amaurosis - Drug Profile
Product Description
Mechanism Of Action
R&D Progress
Gene Therapy to Activate RPGRIP1 for Leber Congenital Amaurosis - Drug Profile
Product Description
Mechanism Of Action
R&D Progress
LX-101 - Drug Profile
Product Description
Mechanism Of Action
R&D Progress
OCU-400 - Drug Profile
Product Description
Mechanism Of Action
R&D Progress
OXB-204 - Drug Profile
Product Description
Mechanism Of Action
R&D Progress
QRX-136 - Drug Profile
Product Description
Mechanism Of Action
R&D Progress
SAR-439483 - Drug Profile
Product Description
Mechanism Of Action
R&D Progress
sepofarsen - Drug Profile
Product Description
Mechanism Of Action
R&D Progress
VAR-002 - Drug Profile
Product Description
Mechanism Of Action
R&D Progress
VAR-003 - Drug Profile
Product Description
Mechanism Of Action
R&D Progress
Leber Congenital Amaurosis (LCA) - Dormant Projects
Leber Congenital Amaurosis (LCA) - Product Development Milestones
Featured News & Press Releases
Jun 23, 2021: Editas Medicine announces enrollment of the first pediatric cohort in the BRILLIANCE clinical trial of EDIT-101 for the treatment of LCA10 following IDMC endorsement
Mar 30, 2021: Variant confirms breakthrough in treatment of hereditary CRX-dependent retinopathies with innovative gene therapy product VAR002
Feb 23, 2021: European Commission grants Ocugen Orphan Medicinal Product Designation for gene therapy product candidate, OCU400, for the treatment of both retinitis pigmentosa and Leber congenital amaurosis
Aug 06, 2020: Editas Medicine regains full global rights to ocular medicines
Mar 04, 2020: Allergan and Editas Medicine announce dosing of first patient in landmark phase 1/2 clinical trial of CRISPR medicine AGN-151587 (EDIT-101) for the treatment of LCA10
Jan 13, 2020: Editas Medicine reports presentation on EDIT-101 at J.P. Morgan Healthcare Conference
Sep 18, 2019: Ocugen granted FDA orphan drug designation for OCU400 (NR2E3) gene therapy for the treatment of CEP290 mutation associated retinal disease
Jul 26, 2019: Allergan and Editas to assess in-vivo CRISPR editing to treat LCA10
Apr 29, 2019: Allergan and Editas Medicine announce initial data from natural history study to evaluate patients with leber congenital amaurosis 10 (LCA10)
Jan 21, 2019: Editas medicine announces publication in nature medicine of data supporting the development of EDIT-101 to treat Leber Congenital Amaurosis 10 (LCA10)
Jan 07, 2019: Editas Medicine reports on recent progress at J.P. Morgan Healthcare Conference
Nov 30, 2018: Editas Medicine Announces FDA Acceptance of IND Application for EDIT-101
Aug 27, 2018: Editas Medicine announces transition of chief medical officer
Aug 16, 2018: Editas Medicine Announces the Completion of the Recombinant DNA Advisory Committee (RAC) Registration Process
May 18, 2018: Editas Medicine Reports Data Demonstrating Subretinal Injection of EDIT-101 Well-tolerated in Non-human Primates
Appendix
Methodology
Coverage
Secondary Research
Primary Research
Expert Panel Validation
Contact Us
Disclaimer

List Of Tables

LIST OF TABLES

Number of Products under Development for Leber Congenital Amaurosis (LCA), 2021
Number of Products under Development by Companies, 2021
Number of Products under Development by Universities/Institutes, 2021
Products under Development by Companies, 2021
Products under Development by Universities/Institutes, 2021
Number of Products by Stage and Target, 2021
Number of Products by Stage and Mechanism of Action, 2021
Number of Products by Stage and Route of Administration, 2021
Number of Products by Stage and Molecule Type, 2021
Leber Congenital Amaurosis (LCA) - Pipeline by Atsena Therapeutics Inc, 2021
Leber Congenital Amaurosis (LCA) - Pipeline by Editas Medicine Inc, 2021
Leber Congenital Amaurosis (LCA) - Pipeline by Generation Bio Co, 2021
Leber Congenital Amaurosis (LCA) - Pipeline by IVERIC bio Inc, 2021
Leber Congenital Amaurosis (LCA) - Pipeline by MeiraGTx Holdings Plc, 2021
Leber Congenital Amaurosis (LCA) - Pipeline by Ocugen Inc, 2021
Leber Congenital Amaurosis (LCA) - Pipeline by Odylia Therapeutics Inc, 2021
Leber Congenital Amaurosis (LCA) - Pipeline by Oxford BioMedica Plc, 2021
Leber Congenital Amaurosis (LCA) - Pipeline by ProQR Therapeutics NV, 2021
Leber Congenital Amaurosis (LCA) - Pipeline by Variant, 2021
Leber Congenital Amaurosis (LCA) - Dormant Projects, 2021

List Of Figures

LIST OF FIGURES

Number of Products under Development for Leber Congenital Amaurosis (LCA), 2021
Number of Products under Development by Companies, 2021
Number of Products under Development by Universities/Institutes, 2021
Number of Products by Targets, 2021
Number of Products by Stage and Targets, 2021
Number of Products by Mechanism of Actions, 2021
Number of Products by Stage and Mechanism of Actions, 2021
Number of Products by Routes of Administration, 2021
Number of Products by Stage and Routes of Administration, 2021
Number of Products by Molecule Types, 2021
Number of Products by Stage and Molecule Types, 2021